Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population

被引：0
|
作者：
Juan Fan
Hua-Yun He
Huan-Huan Li
Pi-Liu Wu
Lei Tang
Bo-Yin Deng
Wen-Hui Dong
Jian-Hui Wang
机构：
[1] Children’s Hospital of Chongqing Medical University,Department of Neonatology
[2] National Clinical Research Center for Child Health and Disorders,Department of Neonatology
[3] Ministry of Education Key Laboratory of Child Development and Disorders,Department of Neonatology
[4] Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity,Department of Pediatrics
[5] Chongqing Jiulongpo People’s Hospital,undefined
[6] Bishan Maternity & Child Hospital of Chongqing,undefined
[7] Affiliated Banan Hospital of Chongqing Medical University,undefined
来源：
BMC Pediatrics | / 24卷
关键词：
Single nucleotide polymorphism; UGT1A1; SLCO1B3; Neonatal hyperbilirubinemia;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [21] SLCO1B1 Polymorphisms are Associated with the Susceptibility to Pulmonary Tuberculosis in Chinese Females
    Li, Wei
    Liu, Wei
    Wang, Xiong
    Dou, Rui
    Zhu, Zunmin
    BIOCHEMICAL GENETICS, 2024, 62 (01) : 385 - 394
  • [22] Influence of organic anion transporting potypeptide(SLCO1B1 and SLCO1B3)genetic polymorphisms on mycophenolic acid in Chinese kidney transplantation patients
    武多娇
    China Medical Abstracts(Surgery), 2011, 20 (04) : 282 - 282
  • [23] Ethnic Differences in the Frequency of Polymorphisms in Influx Transporters SLC10A1, SLC22A1, SLCO1B3, and SLCO1B1
    Dias, Vera
    Ribeiro, Vera
    DRUG METABOLISM REVIEWS, 2009, 41 : 77 - 77
  • [24] Prolonged neutropenia after irinotecan-based chemotherapy in a child with polymorphisms of UGT1A1 and SLCO1B1
    Sakaguchi, S.
    Garcia-Bournissen, F.
    Kim, R.
    Schwarz, U. I.
    Nathan, P. C.
    Ito, S.
    ARCHIVES OF DISEASE IN CHILDHOOD, 2009, 94 (12) : 981 - 982
  • [25] Frequencies of Single-Nucleotide Polymorphisms of SLCO1A2, SLCO1B3 and SLCO2B1 Genes in a Finnish Population
    Laitinen, Alli
    Niemi, Mikko
    BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2011, 108 (01) : 9 - 13
  • [26] Irinotecan/vincristineNeutropenia, constipation and peripheral nerve disorder in a child with polymorphisms of UGT1A1 and SLCO1B1: case report
    Reactions Weekly, 2010, 1290 (1) : 29 - 29
  • [27] Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1
    Chaouch, Leila
    Kalai, Miniar
    Darragi, Imen
    Boudrigua, Imen
    Chaouachi, Dorra
    Ben Ammar, Slim
    Mellouli, F.
    Bjaoui, M.
    Abbes, Salem
    HEMATOLOGY, 2016, 21 (02) : 121 - 125
  • [28] SLCO1B1 polymorphisms and lopinavir plasma concentrations
    Kohlrausch, F. B.
    Estrela, R. de Cassia
    Barroso, P. F.
    Suarez-Kurtz, G.
    PHARMACOGENOMICS, 2010, 11 (07) : 917 - 918
  • [29] The impact of SLCO1B1 genetic polymorphisms on neonatal hyperbilirubinemia: a systematic review with meta-analysis
    Liu, Jiebo
    Long, Jun
    Zhang, Shaofang
    Fang, Xiaoyan
    Luo, Yuyuan
    JORNAL DE PEDIATRIA, 2013, 89 (05) : 434 - 443
  • [30] ABCG2 and SLCO1B1 polymorphisms in the Croatian population
    Karacic, Ena
    Ganoci, Lana
    Simicevic, Livija
    Kirhmajer, Majda Vrkic
    Palic, Jozefina
    Bozina, Tamara
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 307 - 307
12345